Clark W S, Street J S, Feldman P D, Breier A
Lilly Research Laboratories, Indianapolis, Ind 46285, USA.
J Clin Psychiatry. 2001 Jan;62(1):34-40. doi: 10.4088/jcp.v62n0108.
Elderly patients with Alzheimer's disease (AD) commonly exhibit psychotic symptoms, prompting clinicians to administer antipsychotics. This article compares the effects of olanzapine and placebo in the emergence of hallucinations or delusions in AD patients with symptoms of agitation/aggression but little or no psychotic symptomatology at baseline.
A multicenter, double-blind, placebo-controlled study was conducted in nursing home patients with AD according to DSM-IV criteria and symptoms of agitation/aggression and/or psychosis. Patients (N = 206) were randomly assigned to receive either placebo or fixed-dose olanzapine (5, 10, or 15 mg/day) for up to 6 weeks. This article analyzes data from a subgroup of patients (N = 165) with no or minimal delusions and/or hallucinations at baseline as measured by the Neuropsychiatric Inventory-Nursing Home Version (NPI/NH). Three subsets of patients were identified on the basis of their symptoms at baseline: those with no clinically significant hallucinations, those with no clinically significant delusions, and those with no clinically significant delusions or hallucinations.
Of the patients without hallucinations or delusions at baseline (N = 75), the placebo-treated patients showed significantly greater development of these symptoms compared with olanzapine-treated patients overall (NPI/NH hallucinations + delusions mean change score, +2.73 vs. +0.27, p = .006). Similarly, of the patients without baseline hallucinations (N = 153), the placebo-treated patients showed greater hallucinations score increases than did olanzapine-treated patients overall (+1.25 vs. +0.33, p = .026), whereas patients without baseline delusions (N = 87) showed no significant treatment effects. Olanzapine had a favorable safety profile in each patient subset.
These results suggest that, overall, olanzapine effectively attenuated emergence of psychosis in a short-term trial of patients with Alzheimer's disease.
患有阿尔茨海默病(AD)的老年患者通常会出现精神症状,促使临床医生使用抗精神病药物。本文比较了奥氮平和安慰剂对基线时存在激越/攻击症状但几乎没有或没有精神病症状的AD患者出现幻觉或妄想的影响。
根据DSM-IV标准以及激越/攻击和/或精神病症状,对养老院中患有AD的患者进行了一项多中心、双盲、安慰剂对照研究。患者(N = 206)被随机分配接受安慰剂或固定剂量的奥氮平(5、10或15毫克/天),为期6周。本文分析了根据神经精神科问卷-养老院版(NPI/NH)测量,基线时无或仅有极少妄想和/或幻觉的患者亚组(N = 165)的数据。根据患者基线时的症状确定了三个亚组:无临床显著幻觉的患者、无临床显著妄想的患者以及无临床显著妄想或幻觉的患者。
在基线时无幻觉或妄想的患者(N = 75)中,总体而言,接受安慰剂治疗的患者与接受奥氮平治疗的患者相比,这些症状的出现明显更多(NPI/NH幻觉+妄想平均变化得分,+2.73对+0.27,p = 0.006)。同样,在基线时无幻觉的患者(N = 153)中,接受安慰剂治疗的患者幻觉得分的增加幅度大于接受奥氮平治疗的患者总体(+1.25对+0.33,p = 0.026),而基线时无妄想的患者(N = 87)未显示出显著的治疗效果。奥氮平在每个患者亚组中都具有良好的安全性。
这些结果表明,总体而言,在阿尔茨海默病患者的短期试验中,奥氮平有效地减轻了精神病的出现。